Paragangliomas are rare neuroendocrine tumors that arise from chromaffin-containing tissue. Surgical resection and/or radiation are used for locoregional disease, and reduction of tumor burden with systemic therapy is reserved for metastatic disease. Iobenguane I-131, somatostatin analog (octreotide), and Sunitinib are noncytotoxic options for treatment, while cyclophosphamide, vincristine, and dacarbazine (CVD) and temozolomide are often used as initial chemotherapy options as studies have shown that they offer some tumor response. However, there are no randomized clinical trials demonstrating prolonged survival with the use of chemotherapeutics in metastatic cases. Investigation of alternative therapies that provide survival benefit is th...
Pheochromocytoma and paraganglioma (PPGL) have currently only limited treatment options available fo...
ABSTRACT- A paraganglioma is a rare tumor, composed of chromaffin cells, groups of cells associated ...
Malignant pheochromocytomas and paragangliomas affect a very small percentage of the general populat...
There is little evidence to direct the management of malignant paragangliomas (mPGL) beyond initial ...
Paragangliomas are relatively rare chromaffin cell tumors which may be cured through resection. Pati...
AIM: Paragangliomas and pheochromocytomas are rare tumors arising from chromaffin cells. Approximate...
Paragangliomas are neuroendocrine tumors expressing soma-tostatinergic receptors and, thus, may be i...
BACKGROUND: Malignant paragangliomas of the head and neck are very rare tumors of the neuroendocrine...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Malignant paragangliomas pose a real challenge for the practitioners. They are rare complex tumors, ...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Pheochromocytomas and paragangliomas (extra-adrenal pheochromocytomas) are relatively rare catechola...
Malignant phaeochromocytomas are rare tumours accounting for ∼10% of all phaeochromocytomas; the pre...
Multiple spinal and subtentorial intradural paragangliomas were detected in a surgically-treated cau...
Paragangliomas (carotid body tumours, chemodectomas) may arise in any area of the body where sympath...
Pheochromocytoma and paraganglioma (PPGL) have currently only limited treatment options available fo...
ABSTRACT- A paraganglioma is a rare tumor, composed of chromaffin cells, groups of cells associated ...
Malignant pheochromocytomas and paragangliomas affect a very small percentage of the general populat...
There is little evidence to direct the management of malignant paragangliomas (mPGL) beyond initial ...
Paragangliomas are relatively rare chromaffin cell tumors which may be cured through resection. Pati...
AIM: Paragangliomas and pheochromocytomas are rare tumors arising from chromaffin cells. Approximate...
Paragangliomas are neuroendocrine tumors expressing soma-tostatinergic receptors and, thus, may be i...
BACKGROUND: Malignant paragangliomas of the head and neck are very rare tumors of the neuroendocrine...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Malignant paragangliomas pose a real challenge for the practitioners. They are rare complex tumors, ...
Paragangliomas (PGLs) are neuroendocrine tumors that arise embryologically from the neural crest. Sy...
Pheochromocytomas and paragangliomas (extra-adrenal pheochromocytomas) are relatively rare catechola...
Malignant phaeochromocytomas are rare tumours accounting for ∼10% of all phaeochromocytomas; the pre...
Multiple spinal and subtentorial intradural paragangliomas were detected in a surgically-treated cau...
Paragangliomas (carotid body tumours, chemodectomas) may arise in any area of the body where sympath...
Pheochromocytoma and paraganglioma (PPGL) have currently only limited treatment options available fo...
ABSTRACT- A paraganglioma is a rare tumor, composed of chromaffin cells, groups of cells associated ...
Malignant pheochromocytomas and paragangliomas affect a very small percentage of the general populat...